EP0388275B1 - Compositions dermatologiques et cosmétologiques à base d'alcoylcarboxamide et de sel de zinc utiles dans le traitement de la dermite séborrhéique et/ou des troubles de la séborrhée - Google Patents
Compositions dermatologiques et cosmétologiques à base d'alcoylcarboxamide et de sel de zinc utiles dans le traitement de la dermite séborrhéique et/ou des troubles de la séborrhée Download PDFInfo
- Publication number
- EP0388275B1 EP0388275B1 EP90400652A EP90400652A EP0388275B1 EP 0388275 B1 EP0388275 B1 EP 0388275B1 EP 90400652 A EP90400652 A EP 90400652A EP 90400652 A EP90400652 A EP 90400652A EP 0388275 B1 EP0388275 B1 EP 0388275B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- zinc
- process according
- alkylcarboxamide
- seborrheic
- treatment
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 11
- 150000003751 zinc Chemical class 0.000 title claims abstract description 9
- 206010039793 Seborrhoeic dermatitis Diseases 0.000 title claims abstract description 6
- 208000008742 seborrheic dermatitis Diseases 0.000 title claims abstract description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract description 3
- 239000002537 cosmetic Substances 0.000 title 1
- 125000005431 alkyl carboxamide group Chemical group 0.000 claims abstract description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 239000011701 zinc Substances 0.000 claims description 12
- 229910052725 zinc Inorganic materials 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- KOWHWGGCIXBOKF-UHFFFAOYSA-N n-(1-hydroxyethyl)acetamide Chemical compound CC(O)NC(C)=O KOWHWGGCIXBOKF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 235000010755 mineral Nutrition 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 239000011592 zinc chloride Substances 0.000 claims description 2
- 235000005074 zinc chloride Nutrition 0.000 claims description 2
- 239000011670 zinc gluconate Substances 0.000 claims description 2
- 235000011478 zinc gluconate Nutrition 0.000 claims description 2
- 229960000306 zinc gluconate Drugs 0.000 claims description 2
- 229940071566 zinc glycinate Drugs 0.000 claims description 2
- 239000011686 zinc sulphate Substances 0.000 claims description 2
- 235000009529 zinc sulphate Nutrition 0.000 claims description 2
- UOXSXMSTSYWNMH-UHFFFAOYSA-L zinc;2-aminoacetate Chemical compound [Zn+2].NCC([O-])=O.NCC([O-])=O UOXSXMSTSYWNMH-UHFFFAOYSA-L 0.000 claims description 2
- ZSKINHGFQOKUDM-IYEMJOQQSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoic acid;zinc Chemical compound [Zn].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O ZSKINHGFQOKUDM-IYEMJOQQSA-N 0.000 claims 1
- 206010039792 Seborrhoea Diseases 0.000 claims 1
- -1 Zinc lactate Zinc laurate Zinc Chemical compound 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 claims 1
- PIFBJINVDJJYCV-UHFFFAOYSA-J dizinc tetraacetate Chemical compound [Zn+2].[Zn+2].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O PIFBJINVDJJYCV-UHFFFAOYSA-J 0.000 claims 1
- 229940049964 oleate Drugs 0.000 claims 1
- 239000012049 topical pharmaceutical composition Substances 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 229960001763 zinc sulfate Drugs 0.000 description 3
- 229910000368 zinc sulfate Inorganic materials 0.000 description 3
- 241000208690 Hamamelis Species 0.000 description 2
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- IRBDVHUFNSGFOW-UHFFFAOYSA-N n-(1-hydroxypropyl)acetamide Chemical compound CCC(O)NC(C)=O IRBDVHUFNSGFOW-UHFFFAOYSA-N 0.000 description 2
- 229940068886 polyethylene glycol 300 Drugs 0.000 description 2
- 229960003604 testosterone Drugs 0.000 description 2
- 239000004246 zinc acetate Substances 0.000 description 2
- BXCRLBBIZJSWNS-UHFFFAOYSA-N 2-hydroxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCO BXCRLBBIZJSWNS-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 1
- UUQBWZQPSZQOLP-UHFFFAOYSA-N C(C)(C)CC(=O)NC(C)O Chemical compound C(C)(C)CC(=O)NC(C)O UUQBWZQPSZQOLP-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 206010048259 Zinc deficiency Diseases 0.000 description 1
- WHMDKBIGKVEYHS-IYEMJOQQSA-L Zinc gluconate Chemical compound [Zn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O WHMDKBIGKVEYHS-IYEMJOQQSA-L 0.000 description 1
- CANRESZKMUPMAE-UHFFFAOYSA-L Zinc lactate Chemical compound [Zn+2].CC(O)C([O-])=O.CC(O)C([O-])=O CANRESZKMUPMAE-UHFFFAOYSA-L 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000001139 anti-pruritic effect Effects 0.000 description 1
- 239000003908 antipruritic agent Substances 0.000 description 1
- 229940082500 cetostearyl alcohol Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 230000002390 hyperplastic effect Effects 0.000 description 1
- 229940001447 lactate Drugs 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229960003632 minoxidil Drugs 0.000 description 1
- JAFIQQRUEKZCLJ-UHFFFAOYSA-N n-(1-hydroxyethyl)propanamide Chemical compound CCC(=O)NC(C)O JAFIQQRUEKZCLJ-UHFFFAOYSA-N 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 239000011576 zinc lactate Substances 0.000 description 1
- 235000000193 zinc lactate Nutrition 0.000 description 1
- 229940050168 zinc lactate Drugs 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- XLMCDAMBOROREP-UHFFFAOYSA-N zinc;3-phosphonooxypropane-1,2-diolate Chemical compound [Zn+2].OP(O)(=O)OCC([O-])C[O-] XLMCDAMBOROREP-UHFFFAOYSA-N 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/28—Compounds containing heavy metals
- A61K31/315—Zinc compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/30—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
Definitions
- the present invention carried out at the Pierre FABRE Dermatological and Cosmetological Research Center, relates to new topical formulations usable in dermatology and cosmetology.
- formulations based on a combination of alkylcarboxamides and zinc salts, potentiate the anti-inflammatory, antipruritic and antiseborrhoeic effects of the active ingredients.
- the alkylcarboxamide corresponds to the following general formula (I) in which : R represents a hydrogen atom, a C1 to C5 alkyl group or a pyridyl group.
- R1 and R2 may be the same or different and represent a hydrogen atom or a C1 and C5 alkyl group optionally substituted by a hydroxyl.
- These compounds of formula I can be prepared by chemical methods known to those skilled in the art and are mentioned by the applicant in patent 87 12788.
- Alopecic composition comprising Minoxidil (Pierre FABRE, Henri COUSSE and Gilbert MOUZIN).
- alkylcarboxamide corresponding to the following formula (II): in which R1 is a C1 to C5 alkyl group and is preferably the methyl group and more particularly: N (hydroxy 2 ethyl) acetamide N (hydroxy 3 propyl) acetamide N (hydroxy 2 ethyl) propionamide N (hydroxy 2 ethyl) isopropylacetamide
- composition according to the invention advantageously contains from 0.5 to 10% by weight of alkylcarboxamides and from 0.1 to 2% by weight of zinc salts.
- the condition was mainly localized in the face with flaking and pruritus in 39 cases, erythema in 40 cases.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8903235 | 1989-03-13 | ||
FR8903235A FR2644063B1 (fr) | 1989-03-13 | 1989-03-13 | Compositions dermatologiques et cosmetologiques a base d'alcoylcarboxamide et de sel de zinc utiles dans le traitement de la dermite seborrheique et/ou des troubles de la seborrhee |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0388275A1 EP0388275A1 (fr) | 1990-09-19 |
EP0388275B1 true EP0388275B1 (fr) | 1993-02-03 |
Family
ID=9379610
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90400652A Expired - Lifetime EP0388275B1 (fr) | 1989-03-13 | 1990-03-13 | Compositions dermatologiques et cosmétologiques à base d'alcoylcarboxamide et de sel de zinc utiles dans le traitement de la dermite séborrhéique et/ou des troubles de la séborrhée |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0388275B1 (enrdf_load_stackoverflow) |
AT (1) | ATE85219T1 (enrdf_load_stackoverflow) |
DE (1) | DE69000843T2 (enrdf_load_stackoverflow) |
DK (1) | DK0388275T3 (enrdf_load_stackoverflow) |
ES (1) | ES2054283T3 (enrdf_load_stackoverflow) |
FR (1) | FR2644063B1 (enrdf_load_stackoverflow) |
GR (1) | GR3007508T3 (enrdf_load_stackoverflow) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0570405B1 (de) * | 1991-02-06 | 1995-05-24 | Beiersdorf Aktiengesellschaft | Stabile kosmetische mittel |
TW233264B (enrdf_load_stackoverflow) * | 1992-02-03 | 1994-11-01 | Otsuka Pharma Co Ltd | |
FR2710264B1 (fr) * | 1993-09-21 | 1995-12-08 | Rocher Yves Biolog Vegetale | Utilisation pour le traitement des peaux mixtes d'une quantité efficace de substances actives. |
US5599548A (en) * | 1995-05-08 | 1997-02-04 | Elizabeth Arden Co., Division Of Conopco, Inc. | Skin care compositions containing fatty acid amides and retinol or retinyl ester |
FR2740341B1 (fr) * | 1995-10-26 | 1997-12-19 | Oreal | Utilisation de sel de lanthanide, d'etain, de zinc, de manganese, d'yttrium, de cobalt, de baryum, de strontium dans une composition pour la peau |
US5693330A (en) * | 1996-04-25 | 1997-12-02 | Elizabeth Arden Co., Division Of Conopco, Inc. | Skin care compositions containing melinamide and a retinoid |
US5716627A (en) * | 1996-04-25 | 1998-02-10 | Elizabeth Arden Co., Division Of Conopco, Inc. | Skin care compositions containing fatty acid amides, azoles, and retinol or retinyl ester |
US5747051A (en) * | 1996-09-27 | 1998-05-05 | Elizabeth Arden Co., Division Of Conopco, Inc. | Skin care compositions containing an amide of a hydroxy fatty acid and a retinoid |
US5955092A (en) * | 1996-09-27 | 1999-09-21 | Elizabeth Arden Co., Division Of Conopco, Inc. | Skin care compositions containing an n-substituted fatty acid amide and retinol or retinyl ester |
GB0617191D0 (en) * | 2006-08-31 | 2006-10-11 | York Pharma Plc | Improvements in pharmaceutical compositions |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4016287A (en) * | 1972-07-17 | 1977-04-05 | Boehringer Ingelheim Gmbh | Dermatological compositions containing an acylamino-carboxylic acid or an alkyl ester thereof |
ZA752066B (en) * | 1974-05-02 | 1976-03-31 | Draco Ab | Dermatologically active preparation |
FR2599967B1 (fr) * | 1986-06-16 | 1989-03-31 | Bfb Etudes Rech Experimentale | Utilisation de sel de zinc et de la vitamine b6 pour enrayer les processus alopeciques et/ou seborrheiques. |
AU609090B2 (en) * | 1987-02-18 | 1991-04-26 | Milor Scientific, Ltd. | Composition for treatment of acne |
FR2612774B1 (fr) * | 1987-03-27 | 1990-12-28 | Bfb Etudes Rech Experimentale | Compositions cosmetiques et pharmaceutiques, utilisees pour traiter le processus de l'alopecie androgenogenetique, contenant de l'acide azelaique |
-
1989
- 1989-03-13 FR FR8903235A patent/FR2644063B1/fr not_active Expired - Lifetime
-
1990
- 1990-03-13 DE DE9090400652T patent/DE69000843T2/de not_active Expired - Lifetime
- 1990-03-13 AT AT90400652T patent/ATE85219T1/de not_active IP Right Cessation
- 1990-03-13 EP EP90400652A patent/EP0388275B1/fr not_active Expired - Lifetime
- 1990-03-13 ES ES90400652T patent/ES2054283T3/es not_active Expired - Lifetime
- 1990-03-13 DK DK90400652.5T patent/DK0388275T3/da active
-
1993
- 1993-03-30 GR GR930400693T patent/GR3007508T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
DE69000843D1 (de) | 1993-03-18 |
ES2054283T3 (es) | 1994-08-01 |
FR2644063B1 (fr) | 1991-06-14 |
GR3007508T3 (enrdf_load_stackoverflow) | 1993-08-31 |
DE69000843T2 (de) | 1993-07-15 |
FR2644063A1 (fr) | 1990-09-14 |
EP0388275A1 (fr) | 1990-09-19 |
ATE85219T1 (de) | 1993-02-15 |
DK0388275T3 (da) | 1993-03-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0859591B1 (fr) | Utilisation d'au moins un inhibiteur de no-synthase dans le traitement des peaux sensibles | |
EP0738510A2 (fr) | Utilisation d'un inhibiteur d'hmg coenzyme A reductase pour lutter contre le vieillissement de la peau | |
US5045559A (en) | Treatment of skin disorders | |
FR2715845A1 (fr) | Composition cosmétique et/ou dermatologique contenant du vinaigre. | |
EP0388275B1 (fr) | Compositions dermatologiques et cosmétologiques à base d'alcoylcarboxamide et de sel de zinc utiles dans le traitement de la dermite séborrhéique et/ou des troubles de la séborrhée | |
US5258391A (en) | Phenyl alpha acyloxyalkanoic acids, derivatives and their therapeutic use | |
EP0916652B1 (fr) | Nouveaux composés dérivés de n-aryl 2-hydroxy alkylamides | |
US5399785A (en) | Tyrosinase activity inhibitor | |
EP0713696B1 (fr) | Produit pour application topique contenant une lipase et un precurseur d'hydroxyacide | |
US6521222B1 (en) | Inorganic/organic complexes for reducing skin irritation | |
EP1303254A1 (fr) | Composition, notamment cosmetique, comprenant la dhea et/ou un precurseur ou derive de celle-ci, en association avec au moins un inhibiteur de no-synthase | |
JPH0574566B2 (enrdf_load_stackoverflow) | ||
EP0347328B1 (fr) | Composition pour induire et stimuler la croissance des cheveux et/ou freiner leur chute, à base d'un agent tensio-actif amphotère et d'un dérivé pyrimidine | |
FR2807645A1 (fr) | Utilisation d'inhibiteurs de l'alcool deshydrogenase dans le traitement cosmetique des matieres keratiniques | |
EP0223671A1 (fr) | Médicament à action synergétique anti-inflammatoire à base d'un corticostéroide et d'un beta-agoniste | |
CA1325811C (fr) | Derives du norbornane, leur procede de preparation et compositions cosmetique et medicamenteuse les contenant | |
EP0304649B1 (fr) | Sels du piperidino-6, diamino-2,4 pyrimidine oxyde-3 et de dérivés de l'acide thiamorpholinone-3 carboxylique-5, leur utilisation en cosmétique et pharmacie | |
CA2300603C (fr) | Nouveaux composes de la famille des benzylaminodiacetamides, composition les comprenant, procede de preparation et utilisations | |
EP0915857B1 (fr) | Composes de la famille des 3-aryl 2,4 dioxo oxazolidines et leur utilisation en cosmetique et en pharmacie | |
FR2741799A1 (fr) | Utilisation de melatonine dans une composition pour traiter les signes cutanes des etats de fatigue | |
EP0940140A1 (fr) | Composition à base d'alpha-hydroxy-acides et de céramides utilisable par voie topique pour le traitement d'affections dermatologiques | |
JP3270789B2 (ja) | 養毛剤 | |
FR2801508A1 (fr) | Utilisation d'inhibiteurs d'hmg coa-reductase pour le traitement de la seborrhee | |
CA2314539A1 (fr) | Utilisation de l'acide 4,6-dimethoxy-indole 2 -carboxylique ou de ses derives pour le traitement de la seborrhee | |
JP2005501818A (ja) | No−シンターゼインヒビターとしての2−ヘキサデカン酸アスコルビル |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE |
|
17P | Request for examination filed |
Effective date: 19901022 |
|
17Q | First examination report despatched |
Effective date: 19910821 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: PIERRE FABRE COSMETIQUE |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE |
|
REF | Corresponds to: |
Ref document number: 85219 Country of ref document: AT Date of ref document: 19930215 Kind code of ref document: T |
|
REF | Corresponds to: |
Ref document number: 69000843 Country of ref document: DE Date of ref document: 19930318 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
ITF | It: translation for a ep patent filed | ||
K2C2 | Correction of patent specification (partial reprint) published |
Effective date: 19930203 |
|
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 19930416 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: FG4A Free format text: 3007508 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
EPTA | Lu: last paid annual fee | ||
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2054283 Country of ref document: ES Kind code of ref document: T3 |
|
EAL | Se: european patent in force in sweden |
Ref document number: 90400652.5 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 20090218 Year of fee payment: 20 Ref country code: ES Payment date: 20090323 Year of fee payment: 20 Ref country code: DK Payment date: 20090219 Year of fee payment: 20 Ref country code: LU Payment date: 20090325 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20090218 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20090316 Year of fee payment: 20 Ref country code: GB Payment date: 20090303 Year of fee payment: 20 Ref country code: GR Payment date: 20090226 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20090330 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20090312 Year of fee payment: 20 Ref country code: SE Payment date: 20090218 Year of fee payment: 20 Ref country code: FR Payment date: 20090331 Year of fee payment: 20 Ref country code: IT Payment date: 20090319 Year of fee payment: 20 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: V4 Effective date: 20100313 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EUP |
|
BE20 | Be: patent expired |
Owner name: PIERRE *FABRE COSMETIQUE Effective date: 20100313 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 Expiry date: 20100312 |
|
EUG | Se: european patent has lapsed | ||
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20100315 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20100312 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20100315 Ref country code: NL Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20100313 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20100313 |